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Cell Communication and Signaling : CCS
|
November 17, 2023
Epigenetic-focused CRISPR/Cas9 screen identifies (absent, small, or homeotic)2-like protein (ASH2L) as a regulator of glioblastoma cell survival
Ezgi Ozyerli-Goknar, Ezgi Yagmur Kala, Ali Cenk Aksu, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Genome writing to dissect consequences of SVA retrotransposon disease X-Linked Dystonia Parkinsonism
Weimin Zhang, Yu Zhao, Priya Prakash, et al.
Nature Communications
|
March 20, 2024
Oncogenic enhancers prime quiescent metastatic cells to escape NK immune surveillance by eliciting transcriptional memory
Daniela Michelatti, Sven Beyes, Chiara Bernardis, et al.
Cell
|
February 24, 2018
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly
Tatsiana Aneichyk, William T Hendriks, Rachita Yadav, et al.
American Journal of Human Genetics
|
July 30, 2019
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia
Hanneke A Haijes, Maria J E Koster, Holger Rehmann, et al.
Human Mutation
|
October 25, 2019
Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity
Hanyin Cheng, Simona Capponi, Emma Wakeling, et al.
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Search research articles
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Showing results (41-50 of 46) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 46 results.
Cell Communication and Signaling : CCS
|
November 17, 2023
Epigenetic-focused CRISPR/Cas9 screen identifies (absent, small, or homeotic)2-like protein (ASH2L) as a regulator of glioblastoma cell survival
Ezgi Ozyerli-Goknar, Ezgi Yagmur Kala, Ali Cenk Aksu, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Genome writing to dissect consequences of SVA retrotransposon disease X-Linked Dystonia Parkinsonism
Weimin Zhang, Yu Zhao, Priya Prakash, et al.
Nature Communications
|
March 20, 2024
Oncogenic enhancers prime quiescent metastatic cells to escape NK immune surveillance by eliciting transcriptional memory
Daniela Michelatti, Sven Beyes, Chiara Bernardis, et al.
Cell
|
February 24, 2018
Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly
Tatsiana Aneichyk, William T Hendriks, Rachita Yadav, et al.
American Journal of Human Genetics
|
July 30, 2019
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia
Hanneke A Haijes, Maria J E Koster, Holger Rehmann, et al.
Human Mutation
|
October 25, 2019
Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity
Hanyin Cheng, Simona Capponi, Emma Wakeling, et al.
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of 5